Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
  • C08G63/66—Polyesters containing oxygen in the form of ether groups
  • C08G63/668—Polyesters containing oxygen in the form of ether groups derived from polycarboxylic acids and polyhydroxy compounds
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
  • C08G63/68—Polyesters containing atoms other than carbon, hydrogen and oxygen
  • C08G63/685—Polyesters containing atoms other than carbon, hydrogen and oxygen containing nitrogen
  • C08G63/6852—Polyesters containing atoms other than carbon, hydrogen and oxygen containing nitrogen derived from hydroxy carboxylic acids
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
  • C09D167/04—Polyesters derived from hydroxycarboxylic acids, e.g. lactones

Definitions

• This invention relates to polymers, and in particular to curable coating compositions that contain containing polymers.
• Carbamate-functional acrylic pollers are described, for example, in U.S. Pat. No. 5,356,669 and WO 94/10211. These can be prepared by addition polymerization of carbamate-functional acrylic monomers or by transcarbamylation of a hydroxy functional acrylic with an alkyl carbamate.
• Carbamate-functional polyesters prepared by transcarbamylation of a hydroxy-functional polyester, are described in JP 51/4124.
• Hydroxyl functional groups are usually incorporated onto polyester resins by the use of polyol capping agents like trimethylol propane resulting in terminal OH groups, but no pendant OH groups.
• Such resins provide only limited crosslink density upon cure.
• the crosslink density may be increased somewhat by using branched polyesters, which are prepared by the incorporation of trifunctional or higher functional polyols or polyacids in the polyester reaction mixture.
• the degree of branching is often limited due to gelation.
• Low crosslink density in curable polyester resin systems must often be compensated for by using higher molecular weight resins that more closely resemble thermoplastic compositions than thermoset compositions.
• Carbamate-functional polyesters are described in JP 51/4124. This reference describes the preparation of polyesters having carbamate terminal groups by the transesterification of a typical hydroxy-functional polyester with an alkyl carbamate.
• the present invention is directed toward a new method of preparing polyester polymers or oligomers having pendant carbamate groups.
• step (b) reacting the cyclic carbonate group on the half-ester from step (a) with ammonia, ammonium hydroxide, or a primary amine to ring open the cyclic carbonate and form a compound comprising an acid group, a hydroxyl group, and a pendant carbamate group, and
• step (c) reacting a mixture comprising the compound from step (b) and optionally comprising a polyol or a polyacid or both to form the polyester having pendant carbamate groups.
• polyester polymers or oligomers prepared by the above method.
• curable coating compositions comprising the above-described carbamate-functional polyester and a curing agent that is reactive with carbamate.
• Hydroxyalkyl cyclic carbonates useful in the practice of the invention can be prepared by a number of approaches. Certain hydroxyalkyl cyclic carbonates like 3-hydroxypropyl carbonate (i.e., glycerine carbonate) are commercially available. Cyclic carbonate compounds can be synthesized by any of several different approaches. One approach involves reacting an epoxy group-containing compound with CO 2 , preferably under pressure with a catalyst.
• Useful catalysts include any that activate an oxirane ring, such as tertiary amine quaternay salts (e.g., tetramethyl ammonium bromide), tin and/or phosphorous complex salts (e.g., (CH 3 ) 3 SNI:(CH 3 ) 4 PI).
• Epoxides can also be reacted with ⁇ -bytyrolactone in the presence of such catalysts.
• a glycol like glycerine is reacted at temperatures of at least 80° C. (usually under reflux) with diethyl carbonate in the presence of a catalyst (e.g., potassium carbonate) to form a hydroxyalkyl carbonate.
• a functional compound containing a ketal of a 1,2-diol having the structure: ##STR1## can be ring-opened with water at temperatures of at least 60° C., preferably with a trace amount of acid, to form a 1,2-glycol, which is then further reacted with diethyl carbonate to form the cyclic carbonate.
• Cyclic carbonates typically have 5-6-membered rings, as is known in the art. Five-membered rings are preferred, due to their ease of synthesis and greater degree of commercial availability.
• Preferred hydroxyalkyl cyclic carbonates used in the practice can be represented by the formula: ##STR2## where R is a hydroxyalkyl group of 1-18 carbon atoms, preferably 1-6 carbon atoms, and more preferably 1-3 carbon atoms, and n is 1 or 2, which may be substituted by one or more other substituents such as blocked amines or unsaturated groups.
• R is --C m H 2m OH where the hydroxyl may be primary or secondary and m is 1 to 8, and even more preferably, R is --(CH 2 ) p --OH where the hydroxyl is primary and p is 1 to 2.
• the cyclic anhydride that is reacted with the hydroxyalkyl cyclic carbonate can be a monoanhydride or a polyanhydrides that can be reacted with a hydroxyalkyl cyclic carbonate include phthalic anhydride, terephthalic anhydride, trimellitic anhydride, pyromellitic dianhydride, hexahydrophthalic anhydride, methyl hexahydrophthalic anhydride, maleic anhydride, glutamic anhydride, 1,2,4,5-bis-anhydride cyclohexane.
• the anhydride reaction is typically carried out at temperatures under 120° C., preferably under 110° C., and most preferably under 90° C., which can be advantageous because it doesn't subject the carbamate diol to harsh reaction conditions.
• reaction product of the hydroxyalkyl cyclic carbonat compound and the cyclic anhydride compound is itself then reacted with ammonia, ammonium hydroxide, or a primary amine.
• This reaction is performed under mild conditions (e.g., 0°-60° C. in water, methanol, or other known solvents.
• Reaction with ammonia or ammonium hydroxide yields a primary carbamate, and is preferred.
• Reaction with a primary amine yields a secondary (N-substituted) carbamate.
• the ring-opening reaction of ammonia, ammonium hydroxide, or a primary amine with the cyclic carbonate group yields a carbamate group as described above and also a primary or secondary hydroxyl group, which takes part in the polyurethane-forming reaction in the next step of the invention.
• This reaction product thus comprises pendant carbamate groups, and terminal hydroxyl groups.
• the pendant carbamate groups on the polyester of the present invention can be primary or secondary groups.
• Primary carbamate groups can be represented by the formula: ##STR3## and secondary carbamate groups can be represented by the formula: ##STR4## where R is substituted or unsubstituted alkyl of 1-8 carbon atoms, preferably 1-4 carbon atoms, and more preferably 1 carbon atom, or cycloaliphatic. It is to be understood that the terms alkyl and cycloalkyl are to include substituted alkyl and cycloalkyl, such as halogen-substituted alkyl or cycloalkyl or unsaturated group-substituted alkyl.
• a mixture comprising this compound is subjected to conditions for an esterification condensation reaction to form a polyester.
• an esterification condensation reaction it may be beneficial to re-acidify acid groups that were salted by the amine during the ring-opening reaction of the cyclic carbonate group.
• sufficient heat may be applied to dissociate the acid salt and force the esterification reaction.
• Polyesterification reactions are normally carried out at temperatures between 140° C. and 260° C., and for a time ranging from 3 to 15 hours with or without the use of acid esterification catalysts such as phosphorous acid or toluene sulfonic acid present at levels of 0.01 to 2.0 weight percent.
• the reaction is optionally carried out in the presence of a solvent, such as an aromatic hydrocarbon, as is known in the art.
• the reaction may be carried out as a single-stage reaction or as a multistage reaction such as a two-stage reaction.
• the polyesters thus produced generally have a number average molecular weight of from 1000 to 60,000.
• the polyester reaction mixture may comprise one or more polyols and/or one or more polyacids in addition to the compound comprising at least one acid group, at least hydroxyl group, and at least one pendant carbamate group.
• These additional polyols and/or polyacids take part in the esterification condensation reaction that forms the polyester.
• the amounts of these compounds can be adjusted to achieve a polyester with the desired level of functional carbamate groups.
• Polyacids useful in the practice of the invention may contain about 2 to 34 carbon atoms in aliphatic or aromatic moieties, and at least 2, preferably no more than 4, carboxyl groups which may, alternatively, be present in the form of anhydride groups.
• the polyacids may be polyacids themselves or cyclic anhydrides of polyacids, which can be ring opened by the carbamate-containing diol or other polyols during the polyester reaction to form acid groups for polyester condensation.
• polyacids examples include phthalic anhydride, terephthalic acid, isophthalic acid, adipic acid, succinic acid, glutaric acid, fumaric acid, maleic acid, cyclohexane dicarboxylic acid, trimellitic anhydride, azeleic acid, sebasic acid, dimer acid, pyromellitic dianhydride, substituted maleic and fumaric acids such as citraconic, chloromaleic, or mesaconic acids, and substituted succinic acids such as aconitic and iraconic acids. Mixtures of polyacids can be employed.
• Polyols useful in the practice of the invention generally contain more than 2, preferably 2 to about 10 carbon atoms, more preferably about 2 to 8 carbon atoms, in addition to having 2 to about 6, preferably 2 to about 4, hydroxyl groups.
• Some preferred examples of the polyols are one or more of the following: neopentyl glycol, ethylene glycol, propylene glycol, butanediol, hexamethylemediol, 1,2-cyclohexanedimethanol, 1,3-cyclohexanedimethanol, 1,4-cyclohexanedimethanol, trimethylol propane, pentaerythritol, neopentyl glycol hydroxypivalate diethylene glycol, triethylene glycol, tetraethylene glycol, dipropylene glycol, polypropylene glycol, hexylene glycol, 2-methyl-2-ethyl-1,3-propanediol, 2-ethyl-1,3-he
• certain other polyols can be incorporated into the reaction mixture, such as fatty polyols, phenolic polyols (e.g., hydroquinone, phenolphthalein, bisphenol A), oligomeric, or polymeric polyols (e.g., pre-formed polyester polyols).
• phenolic polyols e.g., hydroquinone, phenolphthalein, bisphenol A
• oligomeric e.g., pre-formed polyester polyols
• polymeric polyols e.g., pre-formed polyester polyols
• reaction modifiers e.g., phenolic polyols
• solvents e.g., solvents, dispersing agents, and the like as is known in the art.
• the proportions of the polyacid and polyol, and any other active compounds may be chosen so as to provide an acid-terminated polyester or a hydroxyl-terminated polyester. This can be accomplished by utilizing a stoichiometric excess of polyacid or polyol.
• water-solubility it is important to build water-stabilizing groups into the polyester. This can be accomplished by incorporating water-stabilizing polyether polyols into the reaction mixture so they are incorporated into the polyester or by utilizing dimethanol propionic acid as a polyol in the reaction mixture.
• An intermediate polyester resin may be prepared having hydroxyl or acid terminal groups by the use of an excess of polyacid or polyol component in the polyester reaction mix.
• the terminal groups of the resin may then be controlled by reaction of those terminal groups with an excess of a capping agent, as is known in the art.
• a mono- or multi-functional alcohol may be used to terminate the reaction (cap the free acid groups) at the desired stage (determined by the viscosity and concentration of isocyanate groups present).
• Multi-functional alcohols such as ethylene glycol, trimethylolpropane and hydroxyl-terminated polyesters, can also be employed in this manner.
• the intermediate polyester resin is preferably capped with a monofunctional alcohol (e.g., n-butanol).
• a hydroxyl-terminated intermediate resin can be capped by reaction with an excess of mono- or polyfunctional acid.
• the polyester resin prepared according to the invention can be incorporated into a curable composition such as a coating composition.
• curing is effected by a reaction of the carbamate-functional polyester component with a component (2) that is a compound having a plurality of functional groups that are reactive with the pendant carbamate groups on the polyester.
• Such reactive groups include active methylol or methylalkoxy groups on aminoplast crosslinking agents or on other compounds such as phenol/formaldehyde adducts, siloxane groups, and anhydride groups.
• curing agents include melamine formaldehyde resin (including monomeric or polymeric melamine resin and partially or fully alkylated melamine resin), urea resins (e.g., methylol ureas such as urea formaldehyde resin, alkoxy ureas such as butylated urea formaldehyde resin), polyanhydrides (e.g., polysuccinic anhydride), and polysiloxanes (e.g., trimethoxy siloxane).
• Aminoplast resin such as melamine formaldehyde resin or urea formaldehyde resin are especially preferred.
• a solvent may optionally be utilized in a curable composition used in the practice of the present invention.
• the composition used according to the present invention may be utilized, for example, in the form of substantially solid powder, or a dispersion, it is often desirable that the composition is in a substantially liquid state, which can be accomplished with the use of a solvent.
• This solvent should act as a solvent with respect to both the carbamate-functional polyester as well as the curing agent.
• the solvent can be any organic solvent and/or water.
• the solvent is a polar organic solvent. More preferably, the solvent is a polar aliphatic solvents or polar aromatic solvents.
• the solvent is a ketone, ester, acetate, aprotic amide, aprotic sulfoxide, or aprotic amine.
• useful solvents include methyl ethyl ketone, methyl isobutyl ketone, m-amyl acetate, ethylene glycol butyl ether-acetate, propylene glycol monomethyl ether acetate, xylene, N-methylpyrrolidone, or blends of aromatic hydrocarbons.
• the solvent is water or a mixture of water with small amounts of co-solvents.
• the curable composition used in the practice of the invention may include a catalyst to enhance the cure reaction.
• a catalyst to enhance the cure reaction.
• a strong acid catalyst may be utilized to enhance the cure reaction.
• catalysts are well-known in the art and include, for example, p-toluenesulfonic acid, dinonylnaphthalene disulfonic acid, dodecylbenzenesulfonic acid, phenyl acid phosphate, monobutyl maleate, butyl phosphate, and hydroxy phosphate ester. Strong acid catalysts are often blocked, e.g. with an amine.
• Other catalysts that may be useful in the composition of the invention include Lewis acids, zinc salts, and tin salts.
• the solvent is present in the curable composition in an amount of from about 0.01 weight percent to about 99 weight percent, preferably from about 10 weight percent to about 60 weight percent, and more preferably from about 30 weight percent to about 50 weight percent.
• Coating compositions can be coated on the article by any of a number of techniques well-known in the art. These include, for example, spray coating, dip coating, roll coating, curtain coating, and the like. For automotive body panels, spray coating is preferred.
• any additional agent used for example, surfactants, fillers, stabilizers, wetting agents, dispersing agents, adhesion promoters, UV absorbers, HALS, etc. may be incorporated into the coating composition. While the agents are well-known in the prior art, the amount used must be controlled to avoid adversely affecting the coating characteristics.
• the curable composition according to the invention is preferably utilized in a high-gloss coating and/or as the clearcoat of a composite color-plus-clear coating.
• High-gloss coatings as used herein are coatings having a 20° gloss (ASTM D523-89) or a DOI (ASTM E430-91) of at least 80.
• the curable composition according to the invention can also be used as the basecoat of a composite color-plus-clear coating.
• the pigment may be any organic or inorganic compounds or colored materials, fillers, metallic or other inorganic flake materials such as mica or aluminum flake, and other materials of kind that the art normally names as pigments.
• Pigments are usually used in the composition in an amount of 1% to 100%, based on the total solid weight of components A and B (i.e., a P:B ratio of 0.1 to 1).
• the pigmented basecoat composition may any of a number of types well-known in the art, and does not require explanation in detail herein.
• Polymers known in the art to be useful in basecoat compositions include acrylics, vinyls, polyurethanes, polycarbonates, polyesters, alkyds, and polysiloxanes.
• Preferred polymers include acrylics and polyurethanes.
• the basecoat composition also utilizes a carbamate-functional acrylic polymer.
• Basecoat polymers may be thermoplastic, but are are preferably crosslinkable and comprise one or more type of cross-linkable functional groups.
• Such groups include, for example, hydroxy, isocyanate, amine, epoxy, acrylate, vinyl, silane, and acetoacetate groups. These groups may be masked or blocked in such a way so that they are unblocked and available for the cross-linking reaction under the desired curing conditions, generally elevated temperatures.
• Useful cross-linkable functional groups include hydroxy, epoxy, acid, anhydride, silane, and acetoacetate groups.
• Preferred cross-linkable functional groups include hydroxy functional groups and amino functional groups.
• Basecoat polymers may be self-cross-linkable, or may require a separate cross-linking agent that is reactive with the functional groups of the polymer.
• the cross-linking agent may be an aminoplast resin, isocyanate and blocked isocyanates (including isocyanurates), and acid or anhydride functional cross-linking agents.
• the coating compositions described herein are preferably subjected to conditions so as to cure the coating layers.
• heat-curing is preferred.
• heat curing is effected by exposing the coated article to elevated temperatures provided primarily by radiative heat sources. Curing temperatures will vary depending on the particular blocking groups used in the cross-linking agents, however they generally range between 93° C. and 177° C.
• the compounds according to the present invention are reactive even at relatively low cure temperatures.
• the cure temperature is preferably between 115° C. and 150° C., and more preferably at temperatures between 115° C. and 138° C. for a blocked acid catalyzed system.
• the cure temperature is preferably between 82° C. and 99° C.
• the curing time will vary depending on the particular components used, and physical parameters such as the thickness of the layers, however, typical curing times range from 15 to 60 minutes, and preferably 15-25 minutes for blocked acid catalyzed systems and 10-20 minutes for unblocked acid catalyzed systems.
• Example 1- Preparation of acid functional carbonate intermediate through ring opening of an anhydride with an hydroxy functional carbonate.
• a three neck round bottom flask was fitted with an adapter claisen offset with solvent trap 50 mililiters, condenser, stirrer, nitrogen inlet tube, and thermocouple. This reactor was loaded with the following:
• the agitator was started along with the nitrogen inlet tube, cool water for the condenser, and the batch was heated slowly to 98° C. After the batch reached 98° C., a slight exotherm was noticed and the temperature rose to 105° C. After the exotherm was over, the batch was heated to 110° C. and held at this temperature for 1.5 hours. At this point the reaction was monitored by acid number until the reaction was complete. At the end of the reaction, the reaction product was charged to a 5 liter flask for the ammoniation of the cyclic carbonate.
• the 5 liter three neck flask was fitted with a coldfinger condenser dewar, stirrer, ammonia inlet tube fitted with porous fritted glass tip and thermocouple. This apparatus was then placed in a metal container which was filled with dry ice, water, acetone and sodium chloride as a cold bath in order to control the temperature of the reaction.
• the reactor was then charged with 800 grams of methanol. The temperature of the reaction components were then dropped to 15° C. at which time ammonia gas was bubbled through the reaction until the temperature of the reaction increased to 32° C. At this time, the reaction was stirred and cooled back down to 15° C. This procedure was continued until a carbonate peek was no longer seen in the infrared spectrum. This should take approximately 12 hours depending on the batch size and ammonia concentration.
• the reactor apparatus was converted so that a heated vacuum strip could be performed.
• the vacuum strip was started at room temperature to prevent bumping or over expansion of the system. The temperature was slowly increased (system permitting) to 80° C. under full vacuum 28 in Hg. The vacuum strip was complete when the gas chromatograph was clean of ammonia and methanol. The solids of the reaction were then checked and adjusted with xylene to 53.00% nonvolatile.
• the next step of the reaction was the condensation extension stage of the polyester polyol containing pendant carbamate functionality.
• a three neck round bottom flask was fitted with a perforated 3 plate distilling column, stirrer, adapter claisen with solvent trap 50 mililiters, condenser, nitrogen inlet tube and thermocouple. This reactor was loaded with the following:
• the agitator was turned on, and fifty grams of toluene was charged to the collection trap and slowly heated the reaction to 137.7° C. Once the reaction reaches 137.7° C., the reaction was held at this temperature for three hours (some azeotrope of xylene and water will be seen). After the three-hour hold, the temperature was increased to 170° C. where a very strong azeotrope of xylene and water was observed. The reaction temperature was held at 170° C., for eight hours, at which time the first acid number should be taken. The acid number was then taken every hour until the reaction reached a value between (5-10)AN or (0.089-0.178) miliequivalents per gram. After the reaction was extended to the predetermined acid number, the reaction was cooled to 100° C. At this point any additional solvents are added to bring the solids into specification.

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• 1994
  • 1994-12-21 US US08/361,782 patent/US5508379A/en not_active Expired - Fee Related
• 1995
  • 1995-11-24 MX MX9504906A patent/MX185139B/es unknown
  • 1995-12-09 ES ES95119415T patent/ES2183849T3/es not_active Expired - Lifetime
  • 1995-12-09 EP EP95119415A patent/EP0718337B1/en not_active Expired - Lifetime
  • 1995-12-09 DE DE69528345T patent/DE69528345T2/de not_active Expired - Lifetime
  • 1995-12-12 CA CA002165038A patent/CA2165038A1/en not_active Abandoned
  • 1995-12-20 KR KR1019950053033A patent/KR100351533B1/ko not_active IP Right Cessation
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  • 1995-12-21 JP JP33379795A patent/JP3425283B2/ja not_active Expired - Fee Related
• 2001
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